Four families with loss of function mutations of the thyrotropin receptor

Journal of Clinical Endocrinology and Metabolism

Volumn 81, Issue 12, 1996, Pages 4229-4235

  De Roux, N ^a   Misrahi, M ^a   Brauner, R ^c   Houang, M ^d   Carel, J C ^d   Granier, M ^b   Le Bouc, Y ^d   Ghinea, N ^a   Boumedienne, A ^a   Toublanc, J E ^d   Milgrom, E ^a,e  

^a INSERM   (France)

^b Serv Pediat Neonatologie Hop L   (France)

^c HÔPITAL NECKER ENFANTS MALADES   (France)

^d HÔPITAL SAINT VINCENT DE PAUL   (France)

^e BICÊTRE HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ALANINE; AMINO ACID; ASPARAGINE; ASPARTIC ACID; CYSTEINE; GLUTAMINE; LEUCINE; LIOTHYRONINE; PHENYLALANINE; PROLINE; SERINE; THYROTROPIN RECEPTOR; THYROXINE; TRYPTOPHAN;

ADOLESCENT; ADULT; AMINO ACID SUBSTITUTION; ANIMAL CELL; ARTICLE; BINDING AFFINITY; CASE REPORT; CONTROLLED STUDY; FAMILY STUDY; FEMALE; GENE MUTATION; HORMONE RECEPTOR INTERACTION; HUMAN; MALE; NONHUMAN; PRIORITY JOURNAL; RECEPTOR GENE;

ADENYLATE CYCLASE; ADOLESCENT; ADULT; FEMALE; HUMANS; MALE; MIDDLE AGED; MUTATION; RECEPTORS, THYROTROPIN; THYROTROPIN;

ANIMALIA;

EID: 10544240361     PISSN: 0021972X     EISSN: None     Source Type: Journal    
DOI: 10.1210/jc.81.12.4229     Document Type: Article

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